chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	33895023	33895024	A	G	55	GENIC	homozygous	138303688
8	33895061	33895062	C	T	57	GENIC	homozygous	138303689
8	33895308	33895309	C	T	47	GENIC	homozygous	138303690
8	33895332	33895333	T	C	47	GENIC	homozygous	138303691
8	33896120	33896121	C	T	51	GENIC	homozygous	148733815
8	33896434	33896435	C	T	46	GENIC	homozygous	138303692
8	33896476	33896477	C	T	55	GENIC	homozygous	138303693
8	33896706	33896707	A	G	58	GENIC	homozygous	138303694
8	33896896	33896896		A	43	GENIC	possibly homozygous	138239519
8	33897600	33897607	GACAACT		41	GENIC	homozygous	138239520
8	33897794	33897795	G	A	35	GENIC	homozygous	138303695
8	33898269	33898299	GCTCCTGCTCCTGCTCCTGCTCCTGCTCCT		30	GENIC	homozygous	138239521
8	33902577	33902578	G	A	58	GENIC	homozygous	138303698
8	33903768	33903769	G	A	52	GENIC	homozygous	148733816
8	33903808	33903808		T	41	GENIC	homozygous	138239523
8	33906133	33906133		AAA	8	GENIC	homozygous	138239524
8	33906370	33906371	A	G	39	GENIC	homozygous	148733817
8	33907242	33907243	G	T	31	GENIC	homozygous	138303699
8	33907461	33907462	G	A	59	GENIC	homozygous	148733818
8	33908961	33908963	CA		33	GENIC	homozygous	138239525
8	33909237	33909238	G	T	65	GENIC	homozygous	148733819